Boronic acid, specifically 2-[(2-methoxyethoxy)methyl]phenyl-, is an organic compound characterized by the presence of a boronic acid functional group, which typically features a boron atom bonded to a hydroxyl group and an organic moiety. This compound is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxyethoxy group enhances its solubility and reactivity, allowing it to participate in cross-coupling reactions, such as Suzuki reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, boronic acids are often employed in the development of sensors and drug delivery systems due to their ability to interact selectively with biological molecules. The compound's structure contributes to its stability and reactivity, making it a valuable building block in the synthesis of complex organic molecules. Overall, this boronic acid derivative exemplifies the versatility and utility of boron-containing compounds in modern chemistry.

Boronic acid, [2-[(2-methoxyethoxy)methyl]phenyl]-

858126-53-1: Boronic acid, specifically 2-[(2-methoxyethoxy)methyl]phenyl-, is an organic compound characterized by the presence of a boronic acid functional group, which typically features a boron atom bonded to a hydroxyl group and an organic moiety. This compound is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxyethoxy group enhances its solubility and reactivity, allowing it to participate in cross-coupling reactions, such as Suzuki reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, boronic acids are often employed in the development of sensors and drug delivery systems due to their ability to interact selectively with biological molecules. The compound's structure contributes to its stability and reactivity, making it a valuable building block in the synthesis of complex organic molecules. Overall, this boronic acid derivative exemplifies the versatility and utility of boron-containing compounds in modern chemistry.

CAS 858126-53-1

Boronic acid, [2-[(2-methoxyethoxy)methyl]phenyl]-

2-[(2-methoxyethoxy)methyl]phenylboronic acid

Ref: IN-DA004RBX